Photo credits: ScenTree SAS
Company | Ingredient Name | ID | Naturality | Purity | Latin name | Treated part | Geographical origin | Certifications | Comments | MOQ |
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(R) DELTA DECALACTONE | M_0050449 | Naturel | - | - | - | - | more | - |
General Presentation
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CAS N° : : 705-86-2
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EINECS number : 211-889-1
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FEMA number : 2361
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Density : 0,97
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Optical rotation : Lorem Ipsum
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Allergens : This ingredient does not contain any allergen.
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Refractive Index @20°C : Lorem Ipsum
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Volatility : Base
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Price Range : €€
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Appearance : Colorless liquid
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FLAVIS number : 10.007
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JECFA number : 232
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point : 117°C (à 0,02 mmHg)
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Detection Threshold : 100 ppb (0,00001%)
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Molecular formula : C10H18O2
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Log P : 2,27
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Molecular Weight : 170,25 g/mol
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Fusion Point : -27°C
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Flash Point : 145°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Comparing with other lactones, Delta-Decalactone is without a doubt one of the most coconut-like one, with no real peach effect.
Stability :
Lactones tend to polymerize through time, making them more viscous and leading to a phase shift in alcohol.
Uses in perfumery :
Delta-Decalactone is used for coconut reconstitutions, but also to bring a fruity and milky effect in sandalwood or fruity compositions for example.
Year of discovery :
Data not available.
Isomerism :
Delta-Decalactone has one asymetric carbon. A mixture of its enantiomers is used for perfumery. Delta-Decalactone is a constitutional isomer of Gamma-Decalactone, having one carbon atom less in its cycle, and one more in its ramified carbon chain. The resulting smell is very peachy for the isomer, and coconut-like for Delta-Decalactone.
Synthesis precursor :
Delta-Decalactone is not used for the synthesis of another compound used in perfumery.
Natural availability :
Delta-Decalactone is found in the odorous principle of many fruits as coconut, peach, raspberry, apricot and some cheeses. It does not exist on a natural state for perfumery.
Synthesis route :
Delta-Decalactone can be prepared by oxidation of 2-pentylcyclopentanone, using a peracide.
Regulations & IFRA
This ingredient is not restricted